WO2020098792A1 - 一种正极极片及电化学装置 - Google Patents

一种正极极片及电化学装置 Download PDF

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WO2020098792A1
WO2020098792A1 PCT/CN2019/118844 CN2019118844W WO2020098792A1 WO 2020098792 A1 WO2020098792 A1 WO 2020098792A1 CN 2019118844 W CN2019118844 W CN 2019118844W WO 2020098792 A1 WO2020098792 A1 WO 2020098792A1
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conductive
lithium
battery
pole piece
positive electrode
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PCT/CN2019/118844
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English (en)
French (fr)
Chinese (zh)
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金海族
李振华
李星
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宁德时代新能源科技股份有限公司
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Priority to ES19885692T priority Critical patent/ES2930179T3/es
Priority to EP19885692.4A priority patent/EP3787070B1/en
Priority to US17/057,968 priority patent/US20210135238A1/en
Publication of WO2020098792A1 publication Critical patent/WO2020098792A1/zh

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    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/64—Carriers or collectors
    • H01M4/66—Selection of materials
    • H01M4/665—Composites
    • H01M4/667—Composites in the form of layers, e.g. coatings
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22—Electrodes
    • H01G11/24—Electrodes characterised by structural features of the materials making up or comprised in the electrodes, e.g. form, surface area or porosity; characterised by the structural features of powders or particles used therefor
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22—Electrodes
    • H01G11/26—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22—Electrodes
    • H01G11/26—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features
    • H01G11/28—Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features arranged or disposed on a current collector; Layers or phases between electrodes and current collectors, e.g. adhesives
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22—Electrodes
    • H01G11/30—Electrodes characterised by their material
    • H01G11/32—Carbon-based
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    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
    • H01M10/4235—Safety or regulating additives or arrangements in electrodes, separators or electrolyte
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    • H01M4/06—Electrodes for primary cells
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    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
    • H—ELECTRICITY
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    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/60—Selection of substances as active materials, active masses, active liquids of organic compounds
    • H01M4/602—Polymers
    • H—ELECTRICITY
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    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/624—Electric conductive fillers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/64—Carriers or collectors
    • H01M4/66—Selection of materials
    • H01M4/668—Composites of electroconductive material and synthetic resins
    • H—ELECTRICITY
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    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
    • H01M50/204—Racks, modules or packs for multiple batteries or multiple cells
    • H01M50/207—Racks, modules or packs for multiple batteries or multiple cells characterised by their shape
    • H01M50/209—Racks, modules or packs for multiple batteries or multiple cells characterised by their shape adapted for prismatic or rectangular cells
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M6/00—Primary cells; Manufacture thereof
    • H01M6/14—Cells with non-aqueous electrolyte
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/66—Current collectors
    • H01G11/68—Current collectors characterised by their material
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
    • H01G11/00—Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/66—Current collectors
    • H01G11/70—Current collectors characterised by their structure
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
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    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/021—Physical characteristics, e.g. porosity, surface area
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M2004/026—Electrodes composed of, or comprising, active material characterised by the polarity
    • H01M2004/028—Positive electrodes
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2200/00—Safety devices for primary or secondary batteries
    • H01M2200/10—Temperature sensitive devices
    • H01M2200/106—PTC
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2220/00—Batteries for particular applications
    • H01M2220/10—Batteries in stationary systems, e.g. emergency power source in plant
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2220/00—Batteries for particular applications
    • H01M2220/20—Batteries in motive systems, e.g. vehicle, ship, plane
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00—Road transport of goods or passengers
    • Y02T10/60—Other road transportation technologies with climate change mitigation effect
    • Y02T10/70—Energy storage systems for electromobility, e.g. batteries

Definitions

  • the present application belongs to the field of electrochemical technology. More specifically, the present application relates to a positive pole piece and an electrochemical device including the positive pole piece.
  • Lithium ion batteries are widely used in electric vehicles and consumer electronic products due to their advantages such as high energy density, high output power, long cycle life, and low environmental pollution.
  • lithium-ion batteries are susceptible to fire and explosion when they are subject to abnormal conditions such as crushing, collision, or puncture, causing serious harm. Therefore, the safety of lithium-ion batteries greatly limits the application and popularization of lithium-ion batteries.
  • PTC Positive Temperature Coefficient
  • a PTC material layer (safety coating) is separately provided between the current collector of the battery and the electrode active material layer.
  • the resistance of the PTC material layer increases, thereby increasing the resistance between the current collector and the electrode active material layer, or even powering off, thereby playing a safety role in preventing the electrochemical reaction from continuing.
  • the solvent such as NMP
  • the solvent in the slurry will dissolve the PTC material in the PTC layer and enter the upper active material layer, not only The PTC layer loses the PTC effect and deteriorates the electrical performance.
  • the PTC material layer is easily squeezed to the edge, causing the electrode active material layer to directly contact the current collector, thereby losing the effect of improving safety performance.
  • the performance of the PTC material layer such as response speed and current blocking effect, needs to be greatly improved.
  • An object of the present application is to provide a pole piece and an electrochemical device with improved safety and electrical performance.
  • the present application provides a positive electrode sheet including a current collector, a positive electrode active material layer, and a safety coating disposed between the current collector and the positive electrode active material layer, the safety coating including a polymer matrix, a conductive material, and an inorganic filler , Wherein the polymer matrix is a fluorinated polyolefin and / or chlorinated polyolefin having a cross-linked structure.
  • the weight percentage of the polymer matrix is 35wt% -75wt% (preferably 50wt% -75wt%); the weight percentage of the conductive material It is 5wt% -25wt% (preferably 5wt% -20wt%); the weight percentage of the inorganic filler is 10wt% -60wt% (preferably 15wt% -45wt%).
  • the present application also provides an electrochemical device, which includes the positive pole piece of the present application, and the electrochemical device is preferably a capacitor, a primary battery, or a secondary battery.
  • FIG. 1 is a schematic structural diagram of a positive electrode sheet according to an embodiment of the present application, where 10—current collector; 14—positive electrode active material layer; 12—safety coating (ie, PTC safety coating).
  • 10 current collector
  • 14 positive electrode active material layer
  • 12 safety coating (ie, PTC safety coating).
  • FIG. 2 is a perspective view of an embodiment of a lithium ion battery.
  • FIG. 3 is an exploded view of FIG. 2.
  • FIG. 4 is a perspective view of an embodiment of a battery module.
  • FIG. 5 is a perspective view of an embodiment of a battery pack.
  • Fig. 6 is an exploded view of Fig. 5.
  • FIG. 7 is a schematic diagram of an embodiment of a device using a lithium ion battery as a power source.
  • the present application discloses a positive electrode sheet, including a current collector, a positive electrode active material layer and a safety coating disposed between the current collector and the positive electrode active material layer, the safety coating is a fluorinated polyolefin having a cross-linked structure And / or chlorinated polyolefin polymer matrix, conductive materials and inorganic fillers.
  • Fig. 1 shows a schematic structural view of a positive electrode sheet according to some embodiments of the present application, wherein 10-current collector, 14-positive electrode active material layer, and 12-safety coating (i.e., PTC safety coating).
  • 12-safety coating i.e., PTC safety coating
  • FIG. 1 shows that the PTC safety coating 12 and the positive electrode active material layer 14 are provided only on one side of the positive electrode current collector 10, in other embodiments, the positive electrode current collector 10 may be A PTC safety coating 12 and a positive electrode active material layer 14 are provided on the surface.
  • this application uses a variety of technical means to coordinate processing to improve the performance and stability of the PTC safety coating.
  • the conventional PTC safety coating includes a polymer matrix material, a binder and a conductive material. Its working principle is: at normal temperature, the safety coating relies on a good conductive network formed between conductive materials for electronic conduction; when the temperature increases , The volume of the polymer matrix material begins to expand, the distance between the particles of the conductive material increases, the conductive network is partially blocked, and the resistance of the safety coating gradually increases; and when a certain temperature (such as the operating temperature) is reached, the conductivity The network is almost completely blocked and the current approaches zero, thus protecting the electrochemical device using the safety coating.
  • the solvent such as NMP, etc.
  • electrolyte in the positive electrode active material layer on the upper layer of the safety coating will cause dissolution, swelling and other defects of the polymer material in the safety coating
  • the safety coating will be damaged, affecting the performance of the PTC effect.
  • the inorganic filler is equivalent to a barrier substance, which is beneficial to eliminate the above-mentioned adverse effects of dissolution and swelling, and is conducive to stabilizing the safety coating.
  • the addition of inorganic fillers also helps to ensure that the safety coating is not easily deformed during the compaction of the pole piece. Therefore, the addition of the inorganic filler can well ensure that the safety coating is stably located between the metal current collector and the positive electrode active material layer, and prevent the metal current collector from directly contacting the positive electrode active material layer, thereby improving the safety performance of the battery.
  • the inorganic filler can play the role of stabilizing the safety coating from the following two aspects: (1) hinder the solvent (such as NMP, etc.) in the positive electrode active material layer or the electrolyte from dissolving the polymer material in the safety coating , Swelling and other adverse effects; (2) helps to ensure that the safety coating is not easily deformed during the compaction of the pole piece.
  • hinder the solvent such as NMP, etc.
  • the inventor also unexpectedly found that inorganic fillers can also improve the performance of the safety coating, such as response speed.
  • the working principle of the safety coating is: at normal temperature, the safety coating relies on a good conductive network formed between the conductive materials to conduct electron conduction; when the temperature increases, the volume of the polymer matrix material begins to expand, and between the particles of the conductive material As the spacing increases, the conductive network is partially blocked, and the resistance of the safety coating gradually increases; when a certain temperature (such as actuation temperature) is reached, the conductive network is almost completely blocked, and the current approaches zero.
  • the conductive network is partially restored, so after reaching a certain temperature (such as the operating temperature), the resistance of the safety coating is not as large as expected, and it is still There is very little current.
  • the inorganic filler may be at least one selected from the group consisting of metal oxides, non-metal oxides, metal carbides, non-metal carbides, and inorganic salts, or the conductive carbon coating modification and conductive metal coating modification of the above materials At least one of the modified or conductive polymer coating modified material.
  • the inventor of the present application was surprised to find that the cross-linking treatment can be more beneficial to hinder the adverse effects of the solvent (such as NMP, etc.) or electrolyte in the positive electrode active material layer on the polymer material in the safety coating, such as dissolution and swelling Cracking of the positive electrode active material layer due to uneven stress.
  • the solvent such as NMP, etc.
  • the cross-linking treatment can be achieved by introducing optional activators and cross-linking agents.
  • a strong alkali weak acid salt such as sodium silicate or potassium silicate can be used.
  • the weight ratio of the activator to the polymer matrix is usually 0.5% to 5%.
  • the crosslinking agent may be selected from polyisocyanates (JQ-1, JQ-1E, JQ-2E, JQ-3E, JQ-4, JQ-5, JQ-6, PAPI, emulsifiable MDI, tetraisocyanate) , Polyamines (propylene diamine, MOCA), polyols (polyethylene glycol, polypropylene glycol, trimethylolpropane), glycidyl ether (polypropylene glycol glycidyl ether), inorganic substances (zinc oxide, chloride Aluminum, aluminum sulfate, sulfur, boric acid, borax, chromium nitrate), glyoxal, aziridine, silicones (ethyl orthosilicate, methyl orthosilicate, trimethoxysilane), benzenesulfonic acid ( P-toluenesulfonic acid, p-toluenesulfonyl chloride), ethy
  • the weight ratio of the cross-linking agent to the polymer matrix is 0.01% to 5%. Too little cross-linking agent, the degree of cross-linking of the polymer matrix is low, can not completely eliminate cracking. Too much cross-linking agent may cause gelation during stirring.
  • the activator and the cross-linking agent can be added after the slurry for preparing the safety coating is stirred, and after the cross-linking reaction is performed, the coating is evenly stirred to prepare a safety coating.
  • the performance and stability of the PTC safety coating can be improved, and the electrical performance and safety of the electrochemical device can be improved (especially to improve nail penetration) safety).
  • the safety coating includes a polymer matrix material, a conductive material, an inorganic filler and an optional binder.
  • the components of the safety coating are introduced separately below.
  • the weight percentage of the inorganic filler is usually 10% to 60% by weight. If the content of inorganic filler is too small, it is not enough to stabilize the safety coating; if the content is too large, it will affect the PTC performance of the safety coating.
  • the weight percentage of the inorganic filler is preferably 15% to 45% by weight.
  • the inorganic filler is selected from at least one of metal oxides, non-metal oxides, metal carbides, non-metal carbides, and inorganic salts, or conductive carbon coating modification, conductive metal coating modification of the above materials or The conductive polymer coats at least one of the modified materials.
  • the inorganic filler may be selected from magnesium oxide, alumina, titania, zirconia, silica, silicon carbide, boron carbide, calcium carbonate, aluminum silicate, calcium silicate, potassium titanate, barium sulfate, cobalt acid Lithium, lithium manganate, lithium nickelate, lithium nickel manganate, lithium nickel manganese cobalt oxide, lithium nickel manganese aluminate, lithium iron phosphate, lithium vanadium phosphate, lithium cobalt phosphate, lithium manganese phosphate, lithium iron silicate, silicic acid At least one of lithium vanadium, lithium cobalt silicate, lithium manganese silicate, lithium titanate, or the conductive carbon coating modification, conductive metal coating modification or conductive polymer coating modification of the above materials At least one.
  • the inorganic filler in addition to the above-mentioned role of stabilizing the safety coating (impeding the dissolution and swelling of the organic solvent on the polymer material and ensuring that the safety coating is not easily deformed) and improving the response speed of the safety coating, the inorganic filler In addition to the performance, it can further play the following two roles: (1) improve the overcharge performance of the battery: in the PTC safety coating system composed of a polymer matrix and a conductive material, the electrochemically active material has lithium intercalation and deintercalation The characteristics of ions, so at normal battery operating temperature, electrochemically active materials can be used as "active sites" to participate in the conductive network, that is, the "active sites” in the safety coating increase, during the overcharge process, the electrochemical activity The material will be delithiated and the difficulty of delithiating becomes greater and greater, and the impedance continues to increase.
  • the material of the positive electrode electrochemically active material or the conductive carbon coating modification of the positive electrode electrochemically active material, the conductive metal coating modification or the conductive polymer coating modification is used as the safety coating Inorganic fillers are the most preferred.
  • the positive electrode electrochemically active material is preferably selected from lithium cobaltate, lithium nickel manganese cobaltate, lithium nickel manganese aluminate, lithium iron phosphate, lithium vanadium phosphate, lithium cobalt phosphate, lithium manganese phosphate, lithium iron manganese phosphate, silicic acid Lithium iron, lithium vanadium silicate, lithium cobalt silicate, lithium manganese silicate, spinel lithium manganate, spinel lithium nickel manganate, lithium titanate, or their conductive carbon coating modified materials, At least one of a conductive metal-coated modified material or a conductive polymer-coated modified material.
  • these electrochemically active materials modified by conductive carbon coating such as conductive carbon coated modified lithium cobalt oxide, conductive carbon coated modified nickel manganese lithium cobalt oxide, conductive carbon coated modified nickel manganese Lithium aluminate, conductive carbon coated modified lithium iron phosphate, conductive carbon coated modified lithium vanadium phosphate, conductive carbon coated modified lithium cobalt phosphate, conductive carbon coated modified lithium manganese phosphate, conductive carbon Coated modified lithium iron manganese phosphate, conductive carbon coated modified lithium iron silicate, conductive carbon coated modified lithium vanadium silicate, conductive carbon coated modified lithium cobalt silicate, conductive carbon coated Modified lithium manganese silicate, conductive carbon coated modified spinel lithium manganate, conductive carbon coated modified spinel lithium nickel manganate, conductive carbon coated modified lithium titanate At least one.
  • conductive carbon coated modified lithium cobalt oxide such as conductive carbon coated modified lithium cobalt oxide, conductive carbon coated modified nickel manganese lithium cobalt oxide, conductive carbon coated modified nickel manga
  • electrochemically active materials and conductive carbon-coated modified electrochemically active materials are commonly used materials in the manufacture of lithium batteries, and most of them can be purchased directly through commercial channels.
  • the types of conductive carbon can be graphite, graphene, conductive carbon black, carbon nanotubes, etc.
  • the electrical conductivity of the inorganic filler can be adjusted by adjusting the coating content of the conductive carbon.
  • the average particle diameter D of the inorganic filler in the safety coating satisfies the inorganic in the 100 nm full coating, more preferably 1 ⁇ m ⁇ D ⁇ 6 ⁇ m.
  • the effect of blocking the conductive network at high temperature can also be improved, thereby improving its response speed as a safety coating.
  • the specific surface area (BET) of the inorganic filler in the safety coating layer is not more than 500 m 2 / g.
  • the specific surface area (BET) of the inorganic filler is not more than 500 m 2 / g, a better comprehensive effect can be provided.
  • the conductivity ⁇ of the inorganic filler when the conductivity ⁇ of the inorganic filler satisfies 10 -3 S / m ⁇ 10 2 S / m, it will bring additional benefits.
  • the inorganic filler satisfies the conductivity ⁇ 10 - when 3 S / m ⁇ 10 2 S / m , the coating can be made safe using the conductive properties at normal temperature is improved in the battery.
  • the conductivity of the inorganic filler ⁇ is too small, the initial internal resistance and internal resistance growth rate of the safety coating will be high; if ⁇ is too high, the conductive network will not be easily cut off when the PTC operating temperature is reached, and it may not be able to play a safe role effect. Within the above conductivity range, the internal resistance and internal resistance growth rate of the cell are very small during normal use. When an internal short circuit or high temperature condition occurs, the conductive network can be quickly disconnected.
  • the conductivity ⁇ of certain inorganic fillers does not satisfy 10 -3 S / m ⁇ 10 2 S / m, the conductivity can be made by material modification or modification methods commonly used in the art Meet the above requirements.
  • the functioning principle of the safety coating is: at normal temperature, the safety coating relies on a good conductive network formed between conductive materials to conduct electron conduction; when the temperature increases, the volume of the polymer matrix material begins to expand, The distance between the particles of the conductive material increases, the conductive network is partially blocked, and the resistance of the safety coating gradually increases; and when a certain temperature (such as the operating temperature) is reached, the conductive network is almost completely blocked, and the current approaches zero , Thereby protecting the electrochemical device using the safety coating. Therefore, the amount of conductive material is important for the correct function of the PTC layer.
  • the weight percentage of the conductive material is 5 wt% to 25 wt%, preferably 5 wt% to 20 wt%.
  • the weight ratio of the polymer matrix material to the conductive material is 2 or more.
  • the conductive material may be selected from at least one of a conductive carbon-based material, a conductive metal material, and a conductive polymer material.
  • the conductive carbon-based material may be selected from at least one of conductive carbon black, acetylene black, graphite, graphene, carbon nanotubes, and carbon nanofibers;
  • the conductive metal material may be selected from Al powder, Ni powder, and gold powder At least one of;
  • the conductive polymer material may be selected from at least one of conductive polythiophene, conductive polypyrrole, conductive polyaniline.
  • the conductive material may be used alone or in combination of two or more.
  • the conductive material is usually used in the form of powder or granules. Depending on the specific application environment, its particle size may be 5nm-500nm, such as 10nm-300nm, 15nm-200nm, 15nm-100nm, 20nm-400nm, 20nm-150nm, etc.
  • the polymer matrix material as a safety coating is a polymer matrix material having a cross-linked structure, preferably a fluorinated polyolefin and / or chlorinated polyolefin having a cross-linked structure.
  • the fluorinated polyolefin and / or chlorinated polyolefin refers to polyvinylidene fluoride (PVDF), polyvinylidene chloride (PVDC), modified PVDF, modified PVDC, or any combination thereof, for example, It is selected from PVDF, carboxylic acid modified PVDF, acrylic modified PVDF, PVDF copolymer, PVDC, carboxylic acid modified PVDC, acrylic modified PVDC, PVDC copolymer, or any mixture thereof.
  • the weight percentage of the polymer matrix is 35wt% -75wt%, preferably 40wt% -75wt%, more preferably 50wt% -75wt%.
  • polyethylene, polypropylene or ethylene propylene copolymers are usually used as PTC matrix materials.
  • the material can still function as a PTC thermistor layer, and can help eliminate various problems faced by existing PTC safety coatings. Therefore, it is more preferable to use fluorinated polyolefin and / or chlorinated polyolefin as the polymer matrix material.
  • Fluorinated polyolefins or chlorinated polyolefins are traditionally used more often as binders. When used as a binder, the amount of PVDF is much smaller than the amount of matrix material. For example, PVDF binders in conventional PTC coatings are generally less than 15% or 10%, or even lower relative to the total weight of the coating. In the present application, fluorinated polyolefin or chlorinated polyolefin can be used as a polymer matrix material, and the amount thereof (for example, 35 wt% to 75 wt% relative to the total weight of the safety coating) is much higher than the binder amount.
  • the fluorinated polyolefin and / or chlorinated polyolefin material actually plays two roles, serving as both a PTC matrix and a binder. In this way, the influence of the adhesive on the coating, the response temperature and the response speed of the PTC effect due to the difference between the binder and the PTC matrix material are avoided.
  • the safety coating composed of fluorinated polyolefin and / or chlorinated polyolefin material and conductive material can function as a PTC thermistor layer, with an appropriate operating temperature range, which can be 80 to 160 resistance, so it can be very Improve the high temperature safety performance of the battery.
  • the fluorinated polyolefin and / or chlorinated polyolefin used as the polymer matrix material of the safety coating can be used as both the PTC matrix and the binder, thereby also facilitating the preparation of thinner safety coatings without affecting The adhesion of the safety coating.
  • the solvent (such as NMP, etc.) or electrolyte in the positive electrode active material layer on the upper layer of the safety coating will have adverse effects on the dissolution and swelling of the polymer material in the safety coating.
  • PVDF safety coatings it is easy to cause poor adhesion; for safety coatings with a high content of fluorinated polyolefins and / or chlorinated polyolefins, such adverse effects can be relatively small.
  • the weight percentage of the polymer matrix is 35wt% -75wt%. If the content is too small, the PTC effect of the safety coating cannot be well guaranteed; if the content is too high, the performance of the safety coating, such as response speed, may be affected.
  • the weight percentage of the fluorinated polyolefin and / or chlorinated polyolefin polymer matrix is preferably 40 wt% to 75 wt%, and more preferably 50 wt% to 75 wt%.
  • the safety coating can be formed by conventional methods. For example, by dissolving a polymer matrix material, a conductive material, an inorganic filler, and optional binders or other auxiliary agents (such as crosslinking agents) in a solvent and stirring to form a slurry, and then applying the slurry to a current collector Above, heating and drying can get the required safety coating.
  • the safety coating directly adheres to the current collector and is provided between the current collector and the positive electrode active material layer.
  • the thickness H of the safety coating can be reasonably determined according to actual needs.
  • the thickness H of the safety coating is generally not more than 40 ⁇ m, preferably not more than 25 ⁇ m, and more preferably not more than 20 ⁇ m, 15 ⁇ m or 10 ⁇ m.
  • the coating thickness of the safety coating layer is usually 1 ⁇ m or more, preferably 2 ⁇ m or more, and more preferably 3 ⁇ m or more.
  • the thickness is too small, it is not enough to ensure the effect of the safety coating on improving the safety performance of the battery; if it is too large, it will cause the internal resistance of the battery to increase seriously, thereby affecting the electrochemical performance of the battery during normal operation.
  • the bonding force between the safety coating and the current collector is preferably equal to or greater than 10 N / m.
  • a larger binding force can improve the safety performance of the battery through the nail.
  • the bonding force between the safety coating and the current collector can be increased by introducing an additional binder or by cross-linking the polymer matrix.
  • the polymer matrix is a fluorinated polyolefin and / or chlorinated polyolefin
  • the safety coating is substantially free of polymer matrix materials other than the polymer matrix material Or binder ("substantially free” means content ⁇ indicated content, ⁇ contained content, or ⁇ or ⁇ quantity ⁇ ).
  • the safety coating may additionally contain a binder or other polymer matrix material for enhancing the adhesion between the polymer matrix material and the current collector.
  • the binder may be, for example, PVDF, PVDC, SBR, etc., or may be selected from CMC, polyacrylate, aqueous PVDF, polycarbonate, polyethylene oxide, rubber, polyurethane, sodium carboxymethyl cellulose, Aqueous binders such as polyacrylic acid, acrylonitrile multi-copolymers, gelatin, chitosan, sodium alginate, coupling agents, cyanoacrylates, polymeric cyclic ether derivatives, hydroxy derivatives of cyclodextrins, etc.
  • the polymer matrix used in the safety coating is a fluorinated polyolefin and / or chlorinated polyolefin polymer matrix material
  • the safety coating may be substantially composed of the polymer matrix , Conductive materials and inorganic fillers, that is, other components that do not contain a significant amount (such as content ⁇ molecular, ⁇ ⁇ sub, or ⁇ or ⁇ matrix).
  • the material of the current collector materials commonly used in the art may be used, and metal current collectors such as stainless steel, aluminum, copper, titanium and other metal sheets or metal foils are preferred.
  • the thickness of the metal current collector is 4 ⁇ m to 16 ⁇ m.
  • the elongation at break ⁇ of the current collector is preferably 0.8% ⁇ ⁇ ⁇ 4%. It has been found that if the elongation at break of the current collector is too large, the metal burrs are large when punctured, which is not conducive to improving the safety performance of the battery; otherwise, if the elongation at break of the current collector is too small, it is compacted at the pole piece It is easy to break during processing or when the battery is pressed or collided, which reduces the quality or safety of the battery. Therefore, in order to further improve safety, especially nailing safety, the elongation at break ⁇ of the current collector should be no more than 4% and no less than 0.8%.
  • the elongation at break of the metal current collector can be adjusted by changing the purity, impurity content and additives of the metal current collector, billet production process, rolling speed, heat treatment process, etc.
  • the current collector is a porous aluminum-containing current collector (for example, porous aluminum foil).
  • a porous aluminum-containing current collector for example, porous aluminum foil.
  • the use of porous aluminum foil can reduce the probability of occurrence of metal burrs, and thereby reduce the probability of occurrence of severe aluminothermic reaction, so the safety of the electrochemical device can be further improved.
  • the use of porous aluminum foil can also improve the electrolyte infiltration pole piece, and thus improve the dynamic performance of lithium-ion batteries; and the safety coating can cover the surface of the porous aluminum foil to prevent the upper active material layer in the coating process Leakage phenomenon.
  • the positive electrode active material layer used in the positive electrode sheet of the present application can be selected from various conventional positive electrode active material layers commonly used in the art, and its composition and preparation method are well known in the art and are not particularly limited.
  • the positive electrode active material layer contains a positive electrode active material, and various positive electrode active materials known to those skilled in the art for preparing a positive electrode of a lithium ion secondary battery can be used.
  • the positive electrode active material is a lithium-containing composite metal oxide, specifically
  • the material is, for example, one or more of LiCoO 2 , LiNiO 2 , LiMn 2 O 4 , LiFePO 4 , lithium nickel cobalt manganese oxide (such as LiNi 0.5 Co 0.2 Mn 0.3 O 2 ) and one of lithium nickel manganese oxide kind or several.
  • the positive electrode electrochemically active material (or its coating modified material) is used as the inorganic filler of the safety coating of the positive electrode sheet
  • the positive electrode electrochemically active material in the safety coating and the positive electrode active material layer used in The positive electrode active materials may be the same or different.
  • the negative electrode tab may include a negative electrode current collector and a negative electrode active material layer provided on the negative electrode current collector, and the negative electrode active material layer may include a negative electrode active material, a binder, a conductive material, and the like.
  • the negative electrode active material is, for example, a carbonaceous material such as graphite (artificial graphite or natural graphite), conductive carbon black, carbon fiber, etc., for example, metal or semi-metallic materials such as Si, Sn, Ge, Bi, Sn, In or their alloys, containing lithium Nitride or lithium-containing oxide, lithium metal or lithium aluminum alloy, etc.
  • a carbonaceous material such as graphite (artificial graphite or natural graphite), conductive carbon black, carbon fiber, etc.
  • metal or semi-metallic materials such as Si, Sn, Ge, Bi, Sn, In or their alloys, containing lithium Nitride or lithium-containing oxide, lithium metal or lithium aluminum alloy, etc.
  • the present application also discloses an electrochemical device including the positive pole piece according to the present application.
  • the electrochemical device may be a capacitor, a primary battery, or a secondary battery.
  • it may be a lithium ion capacitor, a lithium ion primary battery, or a lithium ion secondary battery.
  • the construction and preparation methods of these electrochemical devices are known per se.
  • the electrochemical device may have improved safety (such as nail-penetrating safety) and electrical performance.
  • the positive electrode tab of the present application is easy to process, so the manufacturing cost of the electrochemical device using the positive electrode tab of the present application can be reduced.
  • the electrochemical device is a lithium ion battery.
  • FIG. 2 is a perspective view of an embodiment of a lithium ion battery 5.
  • FIG. 3 is an exploded view of FIG. 2. 2 to 3, the lithium ion battery 5 includes a case 51, an electrode assembly 52, a top cover assembly 53, and an electrolyte (not shown).
  • the electrode assembly 52 is accommodated in the case 51.
  • the number of electrode assemblies 52 is not limited, and may be one or more.
  • the electrode assembly 52 includes a positive pole piece, a negative pole piece, and a separator.
  • the separator separates the positive pole piece from the negative pole piece.
  • the electrolyte is injected into the case 51 and impregnates the electrode assembly 52, which includes, for example, a first pole piece, a second pole piece, and a separator.
  • the lithium-ion battery 5 shown in FIG. 2 is a can-type battery, but it is not limited thereto.
  • the lithium-ion battery 5 may be a pouch-type battery, that is, the case 51 is replaced by a metal plastic film and the top cover assembly 53 is eliminated.
  • FIG. 4 is a perspective view of an embodiment of the battery module 4.
  • the battery module 4 provided by the embodiment of the present application includes the lithium ion battery 5 of the present application.
  • the battery module 4 includes a plurality of batteries 5.
  • a plurality of lithium ion batteries 5 are arranged in the longitudinal direction.
  • the battery module 4 can serve as a power source or an energy storage device.
  • the number of lithium ion batteries 5 in the battery module 4 can be adjusted according to the application and capacity of the battery module 4.
  • FIG. 5 is a perspective view of an embodiment of the battery pack 1.
  • Fig. 6 is an exploded view of Fig. 5.
  • the battery pack 1 provided by the present application includes the battery module 4 according to an embodiment of the present application.
  • the battery pack 1 includes an upper case 2, a lower case 3 and a battery module 4.
  • the upper case 2 and the lower case 3 are assembled together and form a space for accommodating the battery module 4.
  • the battery module 4 is placed in the space of the upper case 2 and the lower case 3 assembled together.
  • the output pole of the battery module 4 passes through one or both of the upper case 2 and the lower case 3 to supply power to or charge from the outside.
  • the number and arrangement of battery modules 4 used in the battery pack 1 can be determined according to actual needs.
  • FIG. 7 is a schematic diagram of an embodiment of a device using a lithium ion battery as a power source.
  • the device provided by the present application includes the lithium ion battery 5 according to an embodiment of the present application, and the lithium ion battery 5 can be used as a power source for the device.
  • the device using the lithium ion battery 5 is an electric car.
  • the device using the lithium-ion battery 5 may be any electric vehicle (for example, electric bus, electric tram, electric bicycle, electric motorcycle, electric scooter, electric golf cart, electric truck) other than electric cars ), Electric ships, electric tools, electronic equipment and energy storage systems.
  • the electric vehicle may be an electric pure electric vehicle, a hybrid electric vehicle, or a plug-in hybrid electric vehicle.
  • the device provided in this application may include the battery module 4 described in this application.
  • the device provided in this application may also include the battery pack 1 described in this application.
  • the safety coating is prepared by one of the following two methods.
  • the polymer matrix is not cross-linked:
  • NMP N-methyl-2-pyrrolidone
  • NMP N-methyl-2-pyrrolidone
  • Positive electrode active material layer Then, 90wt% positive electrode active material, 5wt% SP and 5wt% PVDF are mixed with NMP as a solvent, and then evenly coated on the safety coating of the current collector prepared according to the above method; After drying under 85 agents, a positive electrode active material layer is obtained.
  • PVDF manufactured by Manufacturing “Solvay”, model 5130), PVDC;
  • Crosslinking agent tetraisocyanate, polyethylene glycol, acrylonitrile
  • Conductive material conductive agent: Super-P (Swiss TIMCAL company, referred to as SP);
  • Inorganic fillers alumina, lithium iron phosphate (LFP for short), carbon-coated modified lithium iron phosphate (abbreviated as LFP / C), carbon-coated modified lithium titanate (abbreviated as Li 4 Ti 5 O 12 / C);
  • Positive electrode active material NCM811 (LiNi 0.8 Co 0.1 Mn 0.1 O 2 ).
  • the above materials are common and commonly used materials in the field of lithium battery industry, and can be easily obtained through corresponding suppliers through commercial channels.
  • Negative pole piece Add active material graphite, conductive agent Super-P, thickener CMC, adhesive SBR according to the mass ratio of 96.5: 1.0: 1.0: 1.5 to the solvent deionized water and mix to make anode slurry; The slurry is coated on the surface of the negative metal current collector copper foil, and dried at 85 to below, and then trimmed, cut, and slit, and then dried at 110 under vacuum conditions for 4 hours, and the electrode is welded to make The negative pole piece of the secondary battery that meets the requirements.
  • Ethylene carbonate (EC), ethyl methyl carbonate (EMC), and diethyl carbonate (DEC) are mixed in a volume ratio of 3: 5: 2 to obtain an EC / EMC / DEC mixed solvent, and then the fully dried lithium salt LiPF 6 is dissolved in a mixed solvent to obtain a solution with a concentration of 1M, that is, an electrolyte is obtained.
  • the separator Using the polypropylene film made of 12 as the separator, stack the positive pole piece, the separator and the negative pole piece in order, so that the separator is in the middle of the positive pole piece and the negative pole piece to play the role of isolation, and then wound into Bare batteries.
  • Vacuum-bake at 75 ° C for 10 hours inject the electrolyte (prepared as described in "Preparation of Electrolyte” above), vacuum encapsulate and let stand for 24 hours, then charge to 4.2V with a constant current of 0.1C, and then charge at 4.2 Charge at a constant voltage of V until the current drops to 0.05C, then discharge to 3.0V at a constant current of 0.1C, repeat the charge and discharge twice, and finally charge to 3.8V at a constant current of 0.1C, that is, the preparation of the secondary battery is completed.
  • Coating thickness The thickness of the current collector is measured first, and then the total thickness is measured after the coating is applied. The difference between the two is taken as the coating thickness.
  • the absence of cracks in the 100 m 2 pole piece is defined as no cracking.
  • GBT31485-2015 Safety requirements and test methods for power batteries for electric vehicles was used to evaluate the safety of the secondary batteries of the examples and comparative examples, and the test results were recorded.
  • the high temperature resistant steel needle (the cone angle of the needle tip is 45 °), penetrates at a speed of 25mm / s from the direction perpendicular to the battery plate, the penetration position should be close to the geometric center of the puncture surface, the steel needle stays in the battery, Observe whether the battery is burning or exploding.
  • the test conditions for the number of cycles are: at 25 ° C, the secondary battery is subjected to a 1C / 1C cycle test, and the charging and discharging voltage range is 2.8 to 4.2V, and the capacity is reduced to 80% of the first discharge specific capacity to stop the test.
  • the secondary battery was adjusted to 50% SOC with a current of 1C, and the voltage U1 was recorded. Then discharge at a current of 4C for 30 seconds, and record the voltage U2.
  • DCR (U1-U2) / 4C.
  • the DCR of a cell using a non-crosslinked PVDF matrix is used as a reference, recorded as 100%, and the DCR of other cells and its ratio are calculated and recorded.
  • the conventional pole piece P is basically prepared according to the method described in 1.1 "Preparation of the positive pole piece", but no safety coating is provided, that is, the positive electrode active material layer is directly coated on the current collector, and the conventional pole piece N is prepared according to "1.2 negative electrode” Preparation of pole pieces ".
  • Table 1-1 and Table 1-2 show that the introduction of a safety coating using PVDF or PVDC as a polymer matrix greatly improves the needle safety performance of the battery, especially when inorganic fillers are added Significantly. From the DC resistance growth rate data in Table 1-3, it can be seen that the safety coating composed of PVDF and conductive materials does have a PTC effect, and the addition of inorganic fillers significantly improves the DC resistance growth rate of the battery at high temperatures, that is, PTC The effect is more significant.
  • the corresponding safety coating In order to further study the influence of the content of components in the safety coating, the corresponding safety coating, the specific materials and dosages listed in Table 2-1 below are used to prepare the corresponding safety coating, The positive pole piece, the negative pole piece and the battery are tested according to the method specified in the "3. Battery Performance Test" electrical section. In order to ensure the accuracy of the data, 4 batteries of each type (10 batteries for acupuncture test) were prepared and tested independently. The final test results were averaged and summarized in Table 2-2.
  • the weight percentage of the polymer matrix is 35wt% -75wt%
  • the weight percentage of the conductive material is 5wt% -25wt%;
  • the weight percentage of the inorganic filler is 10wt% -60wt%.
  • the content of each component of the safety coating is within the above range, the effect of improving the safety and electrical performance (such as cycle performance) of the battery can be achieved.
  • the cross-linking agent is not added to the pole piece 2-51 to cross-link the polymer matrix, the pole piece cracks and severely cracks.
  • the addition of cross-linking agent has a significant effect on improving the cracking of the pole piece. No cracks occurred in the pole pieces 2-53 to 2-56. Similar experiments with PVDC (pole pieces 2-57 and 2-58) have similar results. It can be seen that the addition of cross-linking agent obviously eliminates the cracking of pole piece coating.
  • the above data shows that PVDF / PVDC can be used as a PTC layer polymer matrix material regardless of cross-linking or not.
  • the resulting battery has high safety (excellent results of acupuncture test experiment), and shows that cross-linking treatment It will have a negative impact on the protective effect of the safety coating.
  • the cross-linking treatment improves the cracking of the pole piece, from severe cracking to no cracking or mild cracking.
  • the cross-linking treatment reduces the swelling of the polymer matrix in the electrolyte, thereby reducing DCR by 15% to 25%, thereby improving the electrical performance of the battery.
  • pole piece of the present application is only illustrated with a lithium battery as an example, but the pole piece of the present application can also be applied to other types of batteries or electrochemical devices, and the Good technical effect.

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3694027A4 (en) * 2017-11-08 2020-12-09 Contemporary Amperex Technology Co., Limited POSITIVE ELECTRODE PLATE, ELECTROCHEMICAL DEVICE AND SAFE COATING

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112447936A (zh) * 2019-08-28 2021-03-05 宁德时代新能源科技股份有限公司 一种负极极片及其锂二次电池
CN111916663B (zh) * 2020-07-27 2022-07-01 珠海冠宇电池股份有限公司 一种正极极片及包括该正极极片的锂离子电池
CN113611872A (zh) * 2020-11-14 2021-11-05 宁德时代新能源科技股份有限公司 电极极片、含有该电极极片的二次电池、电池模块、电池包及用电装置
CN113394405B (zh) * 2021-05-24 2022-07-12 西安交通大学 一种主动防御锂离子电池热失控电极涂层的制备方法
CN114122320B (zh) * 2021-11-25 2023-06-27 珠海冠宇电池股份有限公司 电极片及电化学装置
CN114156434A (zh) * 2021-11-29 2022-03-08 珠海冠宇电池股份有限公司 一种极片和锂离子电池
CN114744206A (zh) * 2022-03-29 2022-07-12 佛山市中技烯米新材料有限公司 一种高安全性的三元锂电池集流体、电极、锂电池
CN114944467B (zh) * 2022-07-01 2024-06-25 珠海冠宇电池股份有限公司 一种极片及包括该极片的电池
CN115820013B (zh) * 2022-07-26 2024-04-12 宁德时代新能源科技股份有限公司 电池外壳及其制备方法、二次电池和用电装置
CN115594872B (zh) * 2022-12-12 2023-03-28 安徽元琛环保科技股份有限公司 一种复合集流体基膜及其制备方法、集流体及其制备方法

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102881861A (zh) * 2012-09-26 2013-01-16 中南大学 一种高温型锂离子电池正极极片
CN106450327A (zh) * 2016-10-13 2017-02-22 中国科学院高能物理研究所 一种辐照提高锂电池聚偏氟乙烯胶黏性能的方法
CN107437622A (zh) * 2016-05-26 2017-12-05 宁德时代新能源科技股份有限公司 电极及其制备方法
KR20180065167A (ko) * 2016-12-07 2018-06-18 주식회사 엘지화학 고분자가 가교된 ptc층을 포함하는 이차전지용 전극 및 이의 제조방법

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6544688B1 (en) * 2000-09-20 2003-04-08 Moltech Corporation Cathode current collector for electrochemical cells
EP1501135B1 (en) * 2003-07-22 2011-06-15 Polymatech Co., Ltd. Thermally conductive holder
JP4339745B2 (ja) * 2003-08-22 2009-10-07 積水化学工業株式会社 合わせガラス及び合わせガラス用中間膜
JP2010238588A (ja) * 2009-03-31 2010-10-21 Daikin Ind Ltd リチウム二次電池の集電積層体
US20120183794A1 (en) * 2009-04-13 2012-07-19 The University Of Vermont And State Agricultural College Whey-protein based environmentally friendly wood adhesives and methods of producing and using the same
KR101768562B1 (ko) * 2010-09-20 2017-08-16 스미토모덴키고교가부시키가이샤 알루미늄 구조체의 제조 방법
CN102176360B (zh) * 2011-02-22 2012-10-10 深圳市长园维安电子有限公司 Ptc热敏电阻及其应用的基材及其制造方法
US9419285B2 (en) * 2012-12-07 2016-08-16 Samsung Electronics Co., Ltd. All-solid battery
TWI550655B (zh) * 2012-12-24 2016-09-21 財團法人工業技術研究院 鋰離子電池及其電極結構
US9273399B2 (en) * 2013-03-15 2016-03-01 Ppg Industries Ohio, Inc. Pretreatment compositions and methods for coating a battery electrode
CN104409681A (zh) * 2014-11-19 2015-03-11 上海航天电源技术有限责任公司 一种含ptc涂层的锂离子电池极片的制备方法
DE102015224967A1 (de) * 2015-12-11 2017-06-14 Robert Bosch Gmbh Batteriemodulgehäuse, Batteriemodul, Batteriepack, Batterie und Fahrzeug sowie Verfahren zum Herstellen eines Batteriemoduls, eines Batteriepacks und einer Batterie
EP3545575A4 (en) * 2016-11-28 2020-08-05 Sila Nanotechnologies Inc. HIGH CAPACITIVE BATTERY ELECTRODES WITH IMPROVED BINDERS, CONSTRUCTION AND PERFORMANCE
JP6729410B2 (ja) * 2017-01-17 2020-07-22 トヨタ自動車株式会社 全固体電池
CN109755463B (zh) * 2017-11-08 2020-12-29 宁德时代新能源科技股份有限公司 一种电极极片、电化学装置及安全涂层
CN109755462B (zh) * 2017-11-08 2021-01-12 宁德时代新能源科技股份有限公司 一种正极极片、电化学装置及安全涂层
CN111200113B (zh) * 2018-11-16 2021-01-12 宁德时代新能源科技股份有限公司 一种正极极片及电化学装置
CN111200111B (zh) * 2018-11-16 2021-03-23 宁德时代新能源科技股份有限公司 一种正极极片及电化学装置

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102881861A (zh) * 2012-09-26 2013-01-16 中南大学 一种高温型锂离子电池正极极片
CN107437622A (zh) * 2016-05-26 2017-12-05 宁德时代新能源科技股份有限公司 电极及其制备方法
CN106450327A (zh) * 2016-10-13 2017-02-22 中国科学院高能物理研究所 一种辐照提高锂电池聚偏氟乙烯胶黏性能的方法
KR20180065167A (ko) * 2016-12-07 2018-06-18 주식회사 엘지화학 고분자가 가교된 ptc층을 포함하는 이차전지용 전극 및 이의 제조방법

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP3787070A4 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3694027A4 (en) * 2017-11-08 2020-12-09 Contemporary Amperex Technology Co., Limited POSITIVE ELECTRODE PLATE, ELECTROCHEMICAL DEVICE AND SAFE COATING
US11349126B2 (en) 2017-11-08 2022-05-31 Contemporary Amperex Technology Co., Limited Positive electrode plate, electrochemical device and safety coating

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